A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620860



Internal ID7007730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81009024..81017921hg38UCSC Ensembl
Innerchr9:81009024..81017921hg38UCSC Ensembl
Outerchr9:81008849..81018089hg38UCSC Ensembl
chr9:83623939..83632836hg19UCSC Ensembl
Innerchr9:83623939..83632836hg19UCSC Ensembl
Outerchr9:83623764..83633004hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg388898
hg198898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13536850
SamplesHG00654
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620860
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer